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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702767Generated: October 30, 2026

Imidazole → HCID 12773635, compound

https://huagongshe.com/reaction/1702767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantHCID 20525194HCID 20525194—
SolventAcetonitrileHCID 6342—
ProductHCID 12773635HCID 1277363562.4%

Reaction Steps

6.1 g (20 mmoles) of crude 4-chloro-4-(2-methyl-phenyl)-4H-indeno[1,2-b]thiophene were taken up in 30 ml of acetonitrile, 4.1 g (60 mmoles) of imidazole were added and the mixture was heated under reflux for 5 hours. The crude product was then precipitated as a syrup by adding 70 ml of water. The supernatant solution was decanted off and the crude product was taken up in ether. The ether solution was dried and evaporated. The residue was taken up in 100 ml of 2 N hydrochloric acid, the insoluble material was separated off and, after cooling, the base was liberated again with sodium hydroxide solution and extracted with ether. The organic phase was dried over sodium sulphate and concentrated. 4.1 g (62.1% of theory) of 4-(imidazol-1-yl)-4-(2-methyl-phenyl)-4H-indeno[1,2-b]thiophene of melting point 75° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04349560
Source datasetuspto-grants-1982_09
ORD IDord-98df74daf3184c66bbcb209359001ca7
Source noteuspto-grants-1982_09